IL30859A - Liquid crystal light valve - Google Patents
Liquid crystal light valveInfo
- Publication number
- IL30859A IL30859A IL30859A IL3085968A IL30859A IL 30859 A IL30859 A IL 30859A IL 30859 A IL30859 A IL 30859A IL 3085968 A IL3085968 A IL 3085968A IL 30859 A IL30859 A IL 30859A
- Authority
- IL
- Israel
- Prior art keywords
- liquid crystal
- mixture
- aminobenzonitrile
- nematic liquid
- weight percent
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
- C09K19/50—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing steroidal liquid crystal compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Liquid Crystal Substances (AREA)
- Liquid Crystal (AREA)
- Steroid Compounds (AREA)
Description
LIQUID CRYSTAL LIGHT VALVE Ti3 s^aa "50 ηκ truroo , Nematic liquid crystal light valves and display devices and nematic liquid crystal compounds useful therein are light valves which are controlled by an electric field. They operate when the liquid crystal material is in its mesomorphic state. Generally, with no electric field applied to the nematic liquid crystal material, the material is slightly turbid in appearance and scatters light to some extent. However, a thin layer of such a material is relatively transparent to light incident thereon. When an electric field above a threshold value, which value depends upon the particular liquid crystal composition, is applied to the layer of liquid crystal material, there is a change in appearance of the layer in the region of the applied field. The layer may appear either brighter or darker to a viewer observing light transmitted through the layer, depending upon the direction of alignment of the liquid crystal molecules in the field with respect to their molecular axes. If the liquid crystal mole-cujes align essentially perpendicular to the direction of the incident light, then additional scattering occurs and that region of the device appears darker to a viewer on. the side of the\device opposite the. source of incident light. If the liquid crystal molecules align with their molecular axes^ essentially parallel to the direction of the incident light, then there is less scattering of the incident light, and that region appears brighter to the viewer." The direction of alignment of the liquid crystal molecules (which in the ■ . : 1 '· ■■.-■ :-\:- '! '.·■:...■,.,;■·. '. . ■■ [ ■ absence of an electric field exist in randomly oriented domains) , in an electric field depends upon the direction of the dipole moment of the molecule with respect to its molecular axis. he electro-o tical effect due t e * panel displays , . in light shutters, and in other applications.
Since the nematic liquid crystal composition' of these devices must be operated while in its nematic mesomorphic state, it is therefore desirable to use compositions which have a lower crystal-nematic translation temperature than prior art compositions. It is also desirable to use composi- ' tions wherein the contrast ratio between an excited or aligned region of the composition and an unexcited or unaligned region of the composition is greater than that achieved in prior art devices.
An electro-optic light valve herein comprises a mixture comprised of a nematic liquid crystal composition of the type whose molecules align in an electric field with at least one member of the group consisting of cholesterol, a cholesterol derivative and a cholesteric liquid crystal.
The light valve includes means for applying an electric field to this mixture . '· . · _ .
FIGURE 1 is a schematic showing of a liquid crystal in its unexcited state; FIGURE 2 is a schematic showing of a liquid crystal in its excited state; and FIGURE 3 is a perspective partially cut-away view of an electro-optic device embodying the invention.
In the absence, of an electric field, a nematic ■„■ liquid crystal composition of the preferred type described herein has its dipole moment essentially parallel to its molecular axis and is believed to have its molecules 11 arranged in small randomly oriented domains, as shown in FIGURE 1, when in its mesomorphic state. Upon the application of a sufficiently high electric field to the liquid crystal . composition, it. is believed that the* domains tend to align , the liquid crystal molecules are aligned essentially parallel to the direction of the applied field. The degree of alignment is a function of the field strength.
In practice, the liquid crystal display includes two planar elements with a. thin liquid crystal film between them. One of the elements is transparent while the other may be transparent, reflective or absorptive depending upon the desired mode of operation of the device. Row conductors and column conductors, which may be transparent conductors, may be applied to a surface of each of the planar elements by applying an electric field to selected areas of the liquid crystal film.
It has been found that by mixing cholesterol, and/or a cholesterol derivative, and/or a cholesteric liquid crystal with a nematic liquid crystal composition of the type whose molecules align in an electric field, one achieves a. mixture which is highly light scattering. The mixture also results in depression of the crystal-nematic transition temperature of the nematic liquid crystals. When an electric field is applied to such a mixture, so as to align the nematic liquid crystal molecules of the mixture with their axes substantially parallel to the direction of the incident light, the mix.ture essentially no longer . scatters the light as it would in its unexcited state and becomes transparent to the incident light. This discovery makes possible light valves and display devices having improved contrast ratios as compared to prior art liquid crystal devices of the type which depend upon alignment of nematic liquid crystal molecules in an electric field.
A preferred embodiment of a novel liquid crystal element is shown in FIGURE 3 in the form of a crossed grid reflective electro-o tic dis la device 30. The novel" device parallel and are separated by a distance of about one-half mil.
On the inner surface 33 of the back plate 31 is an array of parallel spaced conductive back electrode strips 35. On the inner surface 34 of the front plate 32 is an ''array of parallel spaced transparent conductive front electrode strips 36. The front conductive strips 36 are perpendicular to the back conductive strips 35. The outer surface 37 of the back plate 31 coated with a reflective material 38, such as aluminum In the novel device 30, the space between the front and back plates 31 and 32 is filled with a mixture 39 comprising 80 weight percent of a nematic liquid crystal composition and 20 weight percent of cholesterol derivatives. The nematic composition consists essentially of equal weights of p-n -ethoxybenzylidene-_'-aminobenzonitrile and p-n-butoxybenzyli-dene-p_' -aminobenzonitrile . The cholesterol derivatives consist essentially of 23 weight percent of cholesteryl chloride and 77 weight percent of cholesteryl oleate. The mixture may be sealed in the device 30 by using epoxy cement around the edges of the device 30. The nematic composition by itself has a crystal-nematic transition temperature of about 41°C. However, this transition temperature is reduced to about room temperature when mixed with the cholesteryl compounds.
In operation, in its reflective mode, a light source 40 and an observer 41 are both on the same side of the device as the front support plate 32. With no field applied to the device 30, the device 30 appears uniformly bright to the observer 41. When a. dc or ac field of, for example, about 10 volts is applied to any portion of the liquid crystal composition, that portion appears darker then the remainder of the device. Desired or specific portions of the device can ,. ·'■·''· ' k back plate 31 and when the back electrode strips 35 are trans-parent. In this mode, an observer is on the side of the device opposite a light source, and will observe transmitted light rather than reflected light. In this mode of operation, the device appears brighter to the observer in the region of an applied electric field when the incident light is essentially parallel to the direction of the field. This effect is due to the reduction of scattered light upon the application of the electric field and the direct passage of the light to the observer.
As previously stated, the mixtures useful in the practice of this invention include a nematic liquid crystal portion and a portion comprised of either cholesterol, or at least one cholesterol derivative, or at least one cholesteric liquid^crystal , or combinations of these materials. An example of nematic liquid crystal materials of the type in which the molecules align in the direction parallel to the di-rection of an applied electric field are the family of compounds which may be described as £-n-alkoxybenzylidene-p ' -aminobenzonitriles . Mixtures of the compounds p-n -ethoxy-benzylidene-p' -aminobenzonitrile , p-n-butoxybenzylidene-£' -aminobenzonitrile and _-n-octoxybenzylidene -p_' -aminobenzonitrile have been found especially useful in combination with cholesterol, cholesterol derivatives or cholesteric liquid crystals. Mixtures of these compounds combine fast response times due to the large dipole moment of the nematic liquid crystal molecule and also provide reduced crystal-nematic' transition temperatures. With the reduced transition temperatures achieved, devices can be operated at lower temperatures than prior art devices. Preferred weight percent ranges of , '..\ : · > weight percent of £-n-butoxybenzylidene-£' aminobenzonitrile or nematic liquid crystal compositions containing from 15 'to 70 weight percent of each of the three compounds referred to above. The lowest crystal nematic transition temperatures have been found with mixtures comprised of equal weights of _-n-ethoxybenzylidene-p_' -aminobenzonitrile and p_-n-butox-benzylidene-p'-aminobenzonitrile or mixtures comprised of equal weights of £-n-ethoxybenzylidene-£* -aminobenzontrile , £-n-butoxybenzylidene-p' -aminobenzonitrile , and £-n-oxtoxy-benzylidene-p' -aminobenzonitrile . The former composition has a crystal-nematic transition temperature of about 41°C, and the latter composition has a crystal-nematic transition temperature of about 50°C. Both these transition temperatures are depressed to even lower temperatures upon the addition of the cholesteric material to the nematic composition.
These nematic liquid crystal compounds can be prepared by the condensation of p-aminobenzonitrile with the appropriate p-alkoxybenzaldehyde in a refluxing benzene solution with benzenesulfonic acid as a catalyst and azeotropic removal of water. Purification of these compounds is generally accomplished by repeated crystallization from hexane solution to a constant nematic-isotropic transition temperature.
Some examples of other classes of nematic liquid crystal compounds of the type which align in an electric field and which may be combined with cholesteric materials as described herein are: £-alkoxybenzylidene-£' -aminoacylphenones , such as £-butoxybenzylidene-£' -aminoacetophenone ; p-alkl^r-benzoicacid dimers , such as £-butoxybenzoic acid dimer; normal or substituted benzylidene-p-aminoazobenzenes such as benzylidine-£-aminoazobenzene"; 4 ,4"-alkoxynitro-p-terphenyls } such as 4-methox -4"-nitro- -ter henyl ; p- ρ' -alkyldiphenyl- , p-ethylbenzylideneanisidine ; and other compounds such as p ,ρ' -dibenzalbenzidine and p_-butylbenzylidene-_' -amino-phenylbutyrate .
Any cholesterol derivative or cholesteric liquid crystal may be used in the novel mixtures. The table shown below lists some examples of cholesterol derivatives and cholesteric liquid crystals which are useful in the novel device, in combination with the nematic liquid crystal compositions as described above.
TABLE I Cholesterol Derivatives and Cholesteric Liquid Crystals Cholesteryl Oleate (Pract.) Cholesteryl Palmitate Cholesteryl Decanoate Cholesteryl Laurate Cholesteryl Propionate Cholesteryl Heptafluorobuty ate " - . Cholesteryl 2-Furoate Cholesteryl Cinnamate Cholesteryl Cyclohexanecarboxylate Cholesteryl Anisoate . Dicholesteryl Phthalate Cholesteryl p-Nitrobenzoate Cholesteryl p-Phenylazobenzoate Cholesteryl 3 ,5-Dinitrobenzo'ate .
Cholesteryl 2- (2-Ethoxyethoxy)ethyl Carbonate Cholesteryl 2- (2-Methoxyethoxy)ethyl Carbonate Cholesteryl Geranyl Carbonate Cholesteryl Octadecyl Carbonate Cholesteryl 2-Propyn-l-yl Carbonate - - - - - . , ■\: .■·■ Ί' Cholesteryl Methyl Carbonate : Cholesteryl Cinnamyl Carbonate '- Cholesteryl p-Menth-l-en-8-yl Carbonate Cholesteryl Nitrate , Cholestanyl Propynyl Carbonate 38-Chorocholest-5-ene Cholesteryl Methanesulfonate 5a-Cholestan-38-yl Chloroformate Cholesteryl Chloroformate 5a-Cholestan-38-ol Cholesterol ( Stigmasterol It is preferred that the nematic liquid crystal portion of the overall mixture comprise at least 50 weight percent of the total mixture , and preferably from about 75 to 95 weight percent of the. overall mixture. However, it is possible to use mixtures containing as little as 5% nematic liquid crystals and up to 95% of cholesteric material.
The novel mixtures can be prepared by placing the desired proportions of the pure compounds in a vial and heating these compounds until a uniform isotropic, liquid solution is formed. Generally, heating to a temperature of about 100°C. is sufficient. This isotropic liquid is then allowed to cool slowly to room temperature. During cooling the mixture enters its mesomorphic state and, depending upon the particular mixture, may solidify. The novel mixtures can be incorporated into the device by, for example, placing some of the mixture in its mesomorphic state on one support plate and carefully placing the other support plate over the first so that the mixture spreads to form a uniform film between them. Another techni ue is to have the s aced su orts se arated b 'shims
Claims (12)
1. An electro-optic light valve characterized by comprising: a mixture comprised of a nematic liquid crystal composition of the type whose molecules align in an electric field with at least one member of the group consisting of cholesterol, a cholesterol derivative, and a cholesteric liquid crystal, and means for applying an electric field to said mixture . :
2. An electro-optic device according to claim 1 further characterized by comprising: spaced plates at least one of which is transparent to light, said mixture being placed in the space between said plates.
3. The device recited in claim 1 wherein said mixture comprises at least one nematic liquid crystal compound selected from the group consisting of p_-n-ethoxybenzylidene- _' -aminobenzonitrile , p-n-butoxybenzylidene-p' -aminobenzoni- •trile, and £-h-octoxybenzylidene-£' -aminobenzonitrile .
4. The device recited in claim 3 wherein said nematic liquid crystal portion of said mixture comprises between 10 and 90 weight percent of £-n-ethoxybenzylidene-p ' - aminobenzonitrile, and £-n-butoxybenzylidene-p_'-aminobenzoni- trile.
5. The device recited in claim 3 wherein said nematic liquid crystal portion of said mixture comprises between 15 and 75 weight percent of p^-n-ethoxybenzylidene-p' - aminobenzonitrile , £-n-butoxybenzylidene-p' -aminobenzonitrile , and p-n-Qctoxybenzylidene-£' -aminobenzonitrile .
6. The device recited in claim 4 wherein said RCA 59,559
7. The device recited in claim 5 wherein said nematic liquid crystal compounds in said mixture comprises equal weights of p-n-ethoxybenzylidene-p_' -aminobenzonitrile , £-n-butoxybenzylidene-p_' -ajninobenzonitrile , and p-n-octoxy-benzylidene-p' -aminobenzonitrile .
8. The device recited in claim 1 wherein the mixture consists of essentially from 5 to 95 weight percent of nematic liquid crystals and from 5 to 95 weight percent of cholesteric material.
9. The device recited in claim 1 wherein the nematic liquid crystal portion of the mixture comprises from about 75 to 95 weight percent of the mixture.
10. The device recited in claim' 3 wherein the mixture includes from 5 to 30 weight percent of the combination of cholesteryl oleate and cholesteryl chloride.
11. An electro-optic reflective display device according to claim 1 further including a transparent front support plate, a specularly reflective back support plate spaced from and parallel to said front support plate, a I ft plurality of parallel transparent conductive st ps ' on s^aid front support plate , a plurality of parallel conductive strips on said back support plate running in a direction essentially prependicular to said transparent conductive strips on said front support plate and wherein said mixture fills the space between said support.
12. The display device described, in claim 9 wherein said mixture includes at least one nematic liquid crystal compound chosen from the group known as p_-n-alkoxybenzylidene- '-
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68812367A | 1967-12-05 | 1967-12-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
IL30859A0 IL30859A0 (en) | 1968-12-26 |
IL30859A true IL30859A (en) | 1972-07-26 |
Family
ID=24763210
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
IL30859A IL30859A (en) | 1967-12-05 | 1968-10-11 | Liquid crystal light valve |
Country Status (12)
Country | Link |
---|---|
US (1) | US3650603A (en) |
AT (1) | AT287082B (en) |
BE (1) | BE725009A (en) |
CH (1) | CH504008A (en) |
DE (1) | DE1812479A1 (en) |
ES (1) | ES361007A1 (en) |
FR (1) | FR1592944A (en) |
GB (1) | GB1227616A (en) |
IL (1) | IL30859A (en) |
MY (1) | MY7400104A (en) |
NL (1) | NL6817348A (en) |
SE (1) | SE344245B (en) |
Families Citing this family (50)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS523560B1 (en) * | 1971-06-02 | 1977-01-28 | ||
US3736044A (en) * | 1971-06-30 | 1973-05-29 | Ibm | Dispersive acoustical deflector for electromagnetic waves |
DE2222974C3 (en) * | 1972-05-10 | 1978-06-01 | Siemens Ag, 1000 Berlin Und 8000 Muenchen | Image storage screen with a mixture of cholesteric and nematic liquid crystals |
AT314628B (en) * | 1972-07-03 | 1974-04-10 | Elektrovac Fabrikation Elektro | Liquid crystal cell |
US3872050A (en) * | 1972-07-19 | 1975-03-18 | William J Benton | Polyurethane liquid crystal dispersion system and devices |
US3984343A (en) * | 1972-09-29 | 1976-10-05 | General Electric Company | Liquid crystal mixtures with selectively variable dielectric anisotropies |
US3792915A (en) * | 1972-10-17 | 1974-02-19 | Rca Corp | Novel liquid crystal electro-optic devices |
GB1433130A (en) * | 1972-11-09 | 1976-04-22 | Secr Defence | Substituted biphenyl and polyphenyl compounds and liquid crystal materials and devices containing them |
US3837730A (en) * | 1973-11-28 | 1974-09-24 | Bell Telephone Labor Inc | Matrix-addressed liquid crystal display |
JPS605630B2 (en) * | 1973-07-06 | 1985-02-13 | セイコーエプソン株式会社 | display device |
US3936815A (en) * | 1973-08-06 | 1976-02-03 | Nippon Telegraph And Telephone Public Corporation | Apparatus and method for writing storable images into a matrix-addressed image-storing liquid crystal display device |
GB1478592A (en) * | 1974-03-01 | 1977-07-06 | Secr Defence | Liquid crystal devices |
US3989356A (en) * | 1974-02-27 | 1976-11-02 | Gerald Altman | Photographic products for direct observation and optical projection, and photographic processes for their production and utilization, photographic devices for use therewith |
JPS512982Y1 (en) * | 1974-05-01 | 1976-01-28 | ||
DE2504564B2 (en) * | 1974-06-07 | 1977-11-24 | (+) P-ALKOXY-P '- (2-METHYLBUTYL) AZOXYBENZENE AND A CHOLESTERINIC LIQUID CRYSTAL MIXTURE CONTAINING THIS | |
US3973830A (en) * | 1974-06-07 | 1976-08-10 | Matsushita Electric Industrial Co., Ltd. | Electro-optic device |
US3947183A (en) * | 1974-09-25 | 1976-03-30 | Xerox Corporation | Liquid crystal display system |
US4032470A (en) * | 1975-12-22 | 1977-06-28 | Rca Corporation | Electro-optic device |
FR2356173A1 (en) * | 1976-06-21 | 1978-01-20 | Gen Electric | PROCESS FOR IMPROVING THE DESCENT TIME OF A DISPLAY DEVICE COMPOSED OF NEMATIC PROPELLERED LIQUID CRYSTALS |
US4140016A (en) * | 1977-04-07 | 1979-02-20 | Becton, Dickinson And Company | Novel compositions, devices and method |
US4385844A (en) * | 1977-04-07 | 1983-05-31 | Becton, Dickinson And Company | Novel compositions, devices and method |
US4239345A (en) * | 1979-04-16 | 1980-12-16 | Bell Telephone Laboratories, Incorporated | Bistable liquid crystal twist cell |
US4296631A (en) * | 1979-09-21 | 1981-10-27 | Becton, Dickinson And Company | Liquid crystal compositions and devices |
US4493531A (en) * | 1980-07-03 | 1985-01-15 | Control Interface Company Limited | Field sensitive optical displays, generation of fields therefor and scanning thereof |
US4556289A (en) * | 1983-03-21 | 1985-12-03 | Manchester R & D Partnership | Low birefringence encapsulated liquid crystal and optical shutter using same |
CA1241419A (en) * | 1983-08-26 | 1988-08-30 | Paul Milgram | Apparatus for influencing the presentation of visual information |
JPS61198270A (en) * | 1985-02-28 | 1986-09-02 | 富士通株式会社 | Projection type liquid crystal display unit and method and application thereof |
US5453863A (en) * | 1991-05-02 | 1995-09-26 | Kent State University | Multistable chiral nematic displays |
US5847798A (en) * | 1991-05-02 | 1998-12-08 | Kent State University | Polymer stabilized black-white cholesteric reflective display |
US5695682A (en) * | 1991-05-02 | 1997-12-09 | Kent State University | Liquid crystalline light modulating device and material |
US6034753A (en) * | 1991-11-27 | 2000-03-07 | Reveo, Inc. | Circularly polarizing reflective material having super broad-band reflection and transmission characteristics and method of fabricating and using same in diverse applications |
US6753044B2 (en) | 1991-11-27 | 2004-06-22 | Reveo, Inc. | Coloring media having improved brightness and color characteristics |
US5691789A (en) * | 1995-10-30 | 1997-11-25 | Li; Le | Single-layer reflective super broadband circular polarizer and method of fabrication therefor |
ES2129463T3 (en) * | 1992-05-18 | 1999-06-16 | Univ Kent State Ohio | LIGHT MODULATION CRYSTALLINE AND LIQUID DEVICE AND MATERIAL. |
US5251048A (en) * | 1992-05-18 | 1993-10-05 | Kent State University | Method and apparatus for electronic switching of a reflective color display |
KR100320567B1 (en) * | 1992-05-18 | 2002-06-20 | Liquid Crystal Light Modulators & Materials | |
US5463482A (en) * | 1993-10-18 | 1995-10-31 | Raychem Corporation | Liquid crystal composite with droplets of plural chiral nematic materials with different reflection bands |
US5625477A (en) * | 1994-04-11 | 1997-04-29 | Advanced Display Systems, Inc. | Zero field multistable cholesteric liquid crystal displays |
US5668614A (en) * | 1995-05-01 | 1997-09-16 | Kent State University | Pixelized liquid crystal display materials including chiral material adopted to change its chirality upon photo-irradiation |
US5661533A (en) * | 1995-05-19 | 1997-08-26 | Advanced Display Systems, Inc. | Ultra fast response, multistable reflective cholesteric liquid crystal displays |
US6404464B1 (en) | 1995-10-30 | 2002-06-11 | Reveo, Inc. | Method and system for producing color images with improved brightness and color characteristics on radiation absorptive surfaces |
US6774961B2 (en) | 1996-11-08 | 2004-08-10 | Reveo, Inc. | Broad-band polarizer and method of fabricating broad-band polarizers |
US5933203A (en) * | 1997-01-08 | 1999-08-03 | Advanced Display Systems, Inc. | Apparatus for and method of driving a cholesteric liquid crystal flat panel display |
US6034752A (en) * | 1997-03-22 | 2000-03-07 | Kent Displays Incorporated | Display device reflecting visible and infrared radiation |
US6633319B1 (en) | 1998-03-30 | 2003-10-14 | Minolta Co., Ltd. | Image recording apparatus |
US6477464B2 (en) | 2000-03-09 | 2002-11-05 | Donnelly Corporation | Complete mirror-based global-positioning system (GPS) navigation solution |
US6379850B1 (en) * | 1998-06-25 | 2002-04-30 | Minolta Co., Ltd. | Rewritable thermosensible recording material, a production method thereof and a rewritable thermosensible recording medium |
US6515717B1 (en) | 1998-08-28 | 2003-02-04 | Reveo, Inc. | Computer-based system for producing multi-color multilayer images on substrates using dry multi-colored cholesteric liquid crystal (CLC) pigment materials applied to binder material patterns |
US20060066803A1 (en) * | 2004-09-30 | 2006-03-30 | Aylward Peter T | Substrate free flexible liquid crystal displays |
CN101535087B (en) * | 2005-11-01 | 2013-05-15 | 唐纳利公司 | Interior rearview mirror with display |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3322485A (en) * | 1962-11-09 | 1967-05-30 | Rca Corp | Electro-optical elements utilizing an organic nematic compound |
-
1967
- 1967-12-05 US US688123A patent/US3650603A/en not_active Expired - Lifetime
-
1968
- 1968-10-11 IL IL30859A patent/IL30859A/en unknown
- 1968-10-23 SE SE14316/68A patent/SE344245B/xx unknown
- 1968-11-15 GB GB1227616D patent/GB1227616A/en not_active Expired
- 1968-11-25 FR FR1592944D patent/FR1592944A/fr not_active Expired
- 1968-12-03 ES ES361007A patent/ES361007A1/en not_active Expired
- 1968-12-03 DE DE19681812479 patent/DE1812479A1/en active Pending
- 1968-12-04 NL NL6817348A patent/NL6817348A/xx unknown
- 1968-12-05 AT AT1188968A patent/AT287082B/en not_active IP Right Cessation
- 1968-12-05 BE BE725009D patent/BE725009A/xx unknown
- 1968-12-05 CH CH1821268A patent/CH504008A/en not_active IP Right Cessation
-
1974
- 1974-12-30 MY MY104/74A patent/MY7400104A/en unknown
Also Published As
Publication number | Publication date |
---|---|
FR1592944A (en) | 1970-05-19 |
GB1227616A (en) | 1971-04-07 |
IL30859A0 (en) | 1968-12-26 |
DE1812479A1 (en) | 1970-02-19 |
BE725009A (en) | 1969-05-16 |
NL6817348A (en) | 1969-06-09 |
SE344245B (en) | 1972-04-04 |
MY7400104A (en) | 1974-12-31 |
CH504008A (en) | 1971-02-28 |
AT287082B (en) | 1971-01-11 |
US3650603A (en) | 1972-03-21 |
ES361007A1 (en) | 1970-11-16 |
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